With advances in science and technology, our understanding of how the immune system works has never been better. Among them, interferons (IFNs), as an important class of cytokines, play a key role in regulating immune responses. These substances are not only involved in antiviral responses, but are also closely related to various cancers, autoimmune diseases and neurological diseases. In particular, studies using interferon to deliver therapy have demonstrated the potential power and complexity of these factors.
Interferon can be divided into two categories: type 1 interferon (including α, β, etc.) and type 2 interferon (mainly γ). The function of type 1 interferon is mainly to promote the antiviral state of cells and enhance the response ability of the immune system. The receptor for this type of interferon, the interferon α/β receptor (IFNAR), is a ubiquitous cell membrane receptor that can bind to endogenous type 1 interferon and initiate the corresponding signal transduction pathway.
Once secreted, type 1 interferon can act in a paracrine and autocrine manner through IFNAR, initiating the downstream JAK-STAT signaling pathway.
IFNAR consists of two subunits: low-affinity IFNAR1 and high-affinity IFNAR2. These two subunits form a ternary complex after binding to interferon and promote signal transmission.
IFNAR activation triggers transcriptional changes in more than 2,000 genes and affects cell health, apoptosis, autophagy and other processes.
Under normal conditions, levels of type 1 interferon are carefully regulated. This regulation not only depends on the expression of inhibitory signaling elements, but also involves mechanisms such as receptor endocytosis and downregulation. In particular, studies have shown that interferon signaling can respond in different ways to different stimuli, depending on receptor endocytosis.
At this time, positive and negative feedback mechanisms play a key role in the signal transduction of interferon. The expression of negative regulators such as SOCS1 and USP18 is rapidly upregulated after the signal is initiated, thereby reducing the risk of overreaction.
Interferons have a dual effect on the development of many diseases. On the one hand, type 1 interferons are considered to be drivers of multiple autoimmune diseases, and on the other hand, interferons are also used as therapeutic drugs for hematological malignancies and chronic viral infections.
For example, IFNβ is used as the first choice treatment for multiple sclerosis, but its specific mechanism of action is still under investigation.
As research into interferons and their mechanisms of action continues, scientists hope to gain a better understanding of how these biological factors can be used to treat a variety of diseases. At the same time, exploring the performance and response of interferon under different pathological conditions may be one of the hot topics in future medicine. This also raises the question: Can we use the diversity and complexity of interferons to personalize treatments for a wider range of conditions?